Two McLeod patients with novel mutations in XK-Reference-Cited by-同舟云学术

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Two McLeod patients with novel mutations in XK

Published:2011-06 Issue:1-2 Volume:305 Page:160-164
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Dubielecka Patrycja M.,Hwynn Nelson,Sengun Cenk,Lee Soohee,Lomas-Francis Christine,Singer Carlos,Fernandez Hubert H.,Walker Ruth H.

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference30 articles.

1. Point mutations causing the McLeod phenotype;Russo;Transfusion,2002

2. Expression profiles of mouse Kell, XK, and XPLAC mRNA;Lee;J Histochem Cytochem,2007

3. The value of DNA analysis for antigens of the Kell and Kx blood group systems;Lee;Transfusion,2007

4. McLeod phenotype without the McLeod syndrome;Walker;Transfusion,2007

5. Identification and characterization of a novel XK splice site mutation in a patient with McLeod syndrome;Arnaud;Transfusion,2009

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Systematic review of phenotypes in McLeod syndrome and case report of a progressive supranuclear palsy in a female carrier;Orphanet Journal of Rare Diseases;2024-08-25

2. A Novel c.459_460insC Variation in the <i>XK</i> Gene Associated with McLeod Syndrome;Transfusion Medicine and Hemotherapy;2024-07-15

3. Sleep disorders in McLeod syndrome: A case series;Parkinsonism & Related Disorders;2022-09

4. Neuropathology of McLeod Syndrome;Movement Disorders;2021-12-16

5. Unmasking of novel mutations within XK gene that could be used as Diagnostic Markers to Predict McLeod syndrome: Using in silico analysis;2019-02-05

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